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2-carbethoxy-3-phenyl-5-methoxyindan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

154012-99-4

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154012-99-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154012-99-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,0,1 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 154012-99:
(8*1)+(7*5)+(6*4)+(5*0)+(4*1)+(3*2)+(2*9)+(1*9)=104
104 % 10 = 4
So 154012-99-4 is a valid CAS Registry Number.

154012-99-4Relevant academic research and scientific papers

Friedel-Crafts Coordinated Processes: 1-Oxoindanes from Aromatic β-Dicarbonyl Compounds and Aldehydes

Sartori, Giovanni,Bigi, Franca,Maggi, Raimondo,Bernardi, Gian Luca

, p. 7339 - 7342 (1993)

Variously substituted 1-oxoindanes were synthesized by highly selective bis-alkylation of aromatic β-dicarbonyl compounds with non enolizable aldehydes. - Key words: 1-Oxoindanes; β-dicarbonyl chelates; vicinal bis-alkylation.

Indane modulators of glucocorticoid receptor, AP-1, and/or NF/kB activity and use thereof

-

Page/Page column 29, (2008/06/13)

Novel non-steroidal compounds are provided that are useful in treating diseases associated with modulation of the glucocorticoid receptor, AP-1, and/or NF-κB activity including obesity, diabetes, inflammatory and immune diseases having the structure of formula (I): or enantiomers, diastereomers, or a pharmaceutically-acceptable salt, or hydrate, thereof, where X is -A1QA2-; Q is a bond, —C(═O)—, —OC(O)—, —C(═O)NR5—, —SOp—, —SOpNR5—, —C(O)O—, —NR5C(O)—, —OC(O)NR5—, —NR5C(O)O—, —S(O)pNR5C(O)—, —C(O)NR5S(O)p— —NR5S(O)p—, or —NR5C(═O)NR6—. Y is selected from hydrogen, C1-4alkyl, OR16, substituted C1-6alkyl, cycloalkyl, aryl, heterocyclo and heteroaryl. A1 and A2 are independently selected from a bond, C1-3alkylene, or C1-3alkenylene, and R1-R11 are defined herein. Also provided are pharmaceutical compositions, combinations, and methods of treating obesity, diabetes and inflammatory- or immune-associated diseases comprising said compounds.

Selective synthesis of 1-indanones via tandem Knoevenagel condensation-cycloalkylation of β-dicarbonyl compounds and aldehydes

Sartori, Giovanni,Maggi, Raimondo,Bigi, Franca,Porta, Cecilia,Tao, Xiaochun,Bernardi, Gian Luca,Ianelli, Sandra,Nardelli, Mario

, p. 12179 - 12192 (2007/10/02)

Aromatic 1,3-dicarbonyl compounds react with not enolizable aldehydes in the presence of C2H5MgBr or AlCl3 affording 2-carbethoxy- and 2-acetyl-1-indanones via tandem, Knoevenagel condensation-cycloalkylation process.

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